My client has a position available for a Regulatory /Clinical Medical Writer to join their team for a 6-month initial contract within their rare diseases arena.
OUTSIDE IR35
Hybrid, London - 2-3 days WFH
Your new role
As the Regulatory/ Clinical Medical Writer, you will be involved in the authoring of regulatory and clinical documents such as protocols, core dossiers, CSRs, briefing books, responses to questions. QC and light project management (managing timelines), chairing adjudication meetings. You will be an experienced medical writer at developing complex clinical and regulatory documents within the rare disease landscape.
What you'll need to succeed
In order to apply for the Medical Writer contract, you must possess:
- Bachelor's degree in a scientific discipline
- Demonstrated a clear, high-quality scientific writing style in the English language.
- Significant experience in writing regulatory and clinical documents such as protocols, core dossiers, CSRs, briefing books, responses to questions
- Veeva Vault experience
- Great understanding of regulatory guidelines and stats
- Project management skills, consistently achieving multiple tasks and goals on-time.
- Ability to work effectively in a team environment, establish strong collaborative relationships, resolve conflict by creating an atmosphere of openness and trust.
- Able to work with minimal supervision and support.
- Thinks through problems clearly and logically
What you need to do now
Before you apply for this position, it is vital that you are in possession of a UK passport or relevant visa to work without restrictions in the UK and must be based in the UK.
To apply for this position or if you want to discuss other roles that we are working on, please do not hesitate to contact Roberta Atkins on